Tsubaki Haruka, Mendsaikhan Anarmaa, Buyandelger Undral, Tooyama Ikuo, Walker Douglas G
Molecular Neuroscience Research Center, Shiga University of Medical Science, Otsu 520-2192, Japan;
Department of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA.
NeuroSci. 2022 Mar 31;3(2):166-185. doi: 10.3390/neurosci3020013. eCollection 2022 Jun.
Thioredoxin-Interacting Protein (TXNIP) has been shown to have significant pathogenic roles in many human diseases, particularly those associated with diabetes and hyperglycemia. Its main mode of action is to sequester thioredoxins, resulting in enhanced oxidative stress. The aim of this study was to identify if cellular expression of TXNIP in human aged and Alzheimer's disease (AD) brains correlated with pathological structures. This study employed fixed tissue sections and protein extracts of temporal cortex from AD and aged control brains. Studies employed light and fluorescent immunohistochemical techniques using the monoclonal antibody JY2 to TXNIP to identify cellular structures. Immunoblots were used to quantify relative amounts of TXNIP in brain protein extracts. The major finding was the identification of TXNIP immunoreactivity in selective neuronal populations and structures, particularly in non-AD brains. In AD brains, less neuronal TXNIP but increased numbers of TXNIP-positive plaque-associated microglia were observed. Immunoblot analyses showed no significant increase in levels of TXNIP protein in the AD samples tested. In conclusion, this study identified altered patterns of expression of TXNIP in human brains with progression of AD pathology.
硫氧还蛋白相互作用蛋白(TXNIP)已被证明在许多人类疾病中具有重要的致病作用,特别是那些与糖尿病和高血糖相关的疾病。其主要作用方式是螯合硫氧还蛋白,导致氧化应激增强。本研究的目的是确定TXNIP在人类老年大脑和阿尔茨海默病(AD)大脑中的细胞表达是否与病理结构相关。本研究采用了来自AD和老年对照大脑颞叶皮质的固定组织切片和蛋白质提取物。研究采用了使用抗TXNIP单克隆抗体JY2的光镜和荧光免疫组织化学技术来识别细胞结构。免疫印迹法用于量化脑蛋白质提取物中TXNIP的相对含量。主要发现是在选择性神经元群体和结构中鉴定出TXNIP免疫反应性,特别是在非AD大脑中。在AD大脑中,观察到神经元TXNIP减少,但TXNIP阳性斑块相关小胶质细胞数量增加。免疫印迹分析显示,所检测的AD样本中TXNIP蛋白水平没有显著增加。总之,本研究确定了随着AD病理进展,人类大脑中TXNIP表达模式的改变。